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1 .     (20R,22R)-20,22,25-trihydroxy-2 ¦Â,3 ¦Â-(isopropylidenedioxy)-5¦Â-cholest-8(14)-en-6-one
    ÏàËÆ¶È:66.6%
Russian Journal of Organic Chemistry          2010          46          1735-1740
¦¤8(14)-14¦Á-deoxy- and 14¦Á-deoxy-14¦Á-hydroperoxyecdysteroids
A. Sh. Ibragimova, N. A. Ves¡¯kina, I. V. Galyautdinov and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     cumingianol A
C32H54O6     ÏàËÆ¶È:65.6%
Phytochemistry          2011          72          2205-2211
Triterpenes and a triterpene glucoside from Dysoxylum cumingianum
Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Á,12¦Á,16¦Â-Trihydroxy-5¦Â-cholan-24-oic acid
C24H40O5     ÏàËÆ¶È:64.2%
Steroids          2010          75          506-512
Synthesis, aggregation behavior and cholesterol solubilization studies of 16-epi-pythocholic acid (3¦Á,12¦Á,16¦Â-trihydroxy-5¦Â-cholan-24-oic acid)
Nonappa, Uday Maitra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3,20,24,25-tetrahydroxydammarane
C30H54O4     ÏàËÆ¶È:63.3%
Phytochemistry          2004          65          2173-2176
Insect antifeedant compounds from Nothofagus dombeyi and N. pumilio
Odile Thoison, Thierry S¨¦venet, Hermann M. Niemeyer, Graeme B. Russell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     panicualtin D
C32H52O7     ÏàËÆ¶È:63.3%
Journal of the Indian Chemical Society          1999          76          575-581
Study of the stereochemistry of new tetranortriterpenoids isolated from root-wood of Chisocheton paniculatus Hiern(Meliaceae)
R.D.Yadav,J.C.S.Kataky and R.K.Mathur
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Cumingianol B
C32H54O6     ÏàËÆ¶È:62.5%
Phytochemistry          2011          72          2205-2211
Triterpenes and a triterpene glucoside from Dysoxylum cumingianum
Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Cumingianol C
C32H52O5     ÏàËÆ¶È:62.5%
Phytochemistry          2011          72          2205-2211
Triterpenes and a triterpene glucoside from Dysoxylum cumingianum
Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     paniculatin-D
C32H52O7     ÏàËÆ¶È:62.5%
Indian Journal of Chemistry Section B          1999          38B          1359-1363
New protolimonoids and limonoidsart I-isolation,structure elucidation of new protolimonoids and limonoid from the root wood of Chisocheton paniculatus Hiern(Meliaceae)
R D Yadav, J C S Kataky&R K mathur
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Kadpolysperin C
C32H50O5     ÏàËÆ¶È:62.5%
Tetrahedron          2012          68          4820-4829
Kadpolysperins A¨CN, lanostane triterpene acids possessing rich structure types from Kadsura polysperma
Ke Dong, Jian-Xin Pu, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Wei Zhao, Yan Li, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2014-05-26 09:29:36
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